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- AGER J. A., LEHMANN H. Observations on some fast haemoglobins: K, J, N, and Bart's. Br Med J. 1958 Apr 19;1(5076):929–931. doi: 10.1136/bmj.1.5076.929. [DOI] [PMC free article] [PubMed] [Google Scholar]
- AKSOY M., LEHMANN H. Sickle-cell-thalassaemia disease in South Turkey. Br Med J. 1957 Mar 30;1(5021):734–738. doi: 10.1136/bmj.1.5021.734. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ATWATER J., SCHWARTZ I. R., ERSLEV A. J., MONTGOMERY T. L., TOCANTINS L. M. Sickling of erythrocytes in a patient with thalassemia-hemoglobin-I disease. N Engl J Med. 1960 Dec 15;263:1215–1223. doi: 10.1056/NEJM196012152632402. [DOI] [PubMed] [Google Scholar]
- BINGLE J. P., HUEHNS E. R., PRANKERD T. A. Haemoglobin-H disease. Br Med J. 1958 Dec 6;2(5109):1389–1390. doi: 10.1136/bmj.2.5109.1389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BOYER S. H., RUCKNAGEL D. L., WEATHERALL D. J., WATSON-WILLIAMS E. J. FURTHER EVIDENCE OF LINKAGE BETWEEN THE BETA AND DELTA LOCI GOVERNING HUMAN HEMOGLOBIN AND THE POPULATION DYNAMICS OF LINKED GENES. Am J Hum Genet. 1963 Dec;15:438–448. [PMC free article] [PubMed] [Google Scholar]
- CHERNOFF A. I., LIU J. C. The amino acid composition of hemoglobin. II. Analytical technics. Blood. 1961 Jan;17:54–70. [PubMed] [Google Scholar]
- CHERNOFF A. I., MINNICH V., NANAKORN S., TUCHINDA S., KASHEMSANT C., BANGKOK, THAILAND, CHERNOFF R. R. Studies on hemoglobin E. I. The clinical, hematologic, and genetic characteristics of the hemoglobin E syndromes. J Lab Clin Med. 1956 Mar;47(3):455–489. [PubMed] [Google Scholar]
- CHOREMIS C., ZANNOS-MARIOLEA L., AGER J. A., LEHMANN H. Persistence of haemoglobin "Bart's" beyond infancy in a child with thalassaemia. Br Med J. 1959 Sep 5;2(5148):348–349. doi: 10.1136/bmj.2.5148.348. [DOI] [PMC free article] [PubMed] [Google Scholar]
- COHEN F., ZUELZER W. W., NEEL J. V., ROBINSON A. R. Multiple inherited erythrocyte abnormalities in an American Negro family: hereditary spherocytosis, sickling and thalassemia. Blood. 1959 Jul;14(7):816–827. [PubMed] [Google Scholar]
- DITTMAN W. A., HAUT A., WINTROBE M. M., CARTWRIGHT G. E. Hemoglobin H associated with an uncommon variant of thalassemia trait. Blood. 1960 Jul;16:975–983. [PubMed] [Google Scholar]
- DORMANDY K. M., LOCK S. P., LEHMANN H. Haemoglobin Q-alpha-thalassaemia. Br Med J. 1961 Jun 3;1(5239):1582–1585. doi: 10.1136/bmj.1.5239.1582. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ENG LIL, HIN P. S., KENG K. L., ENDENBURG P. M. Chronic hypochromic microcytic anaemia associated with haemoglobin H. Acta Haematol. 1957 Aug;18(2):156–167. doi: 10.1159/000205313. [DOI] [PubMed] [Google Scholar]
- ENG L. L., TJIANG T. G., KENG K. L. Splenectomy in a case of chronic haemolytic anaemia associated with haemoglobin H. J Trop Med Hyg. 1961 Jun;64:136–139. [PubMed] [Google Scholar]
- FESSAS P., PAPASPYROU A. New fast hemoglobin associated with thalassemia. Science. 1957 Nov 29;126(3283):1119–1119. doi: 10.1126/science.126.3283.1119. [DOI] [PubMed] [Google Scholar]
- GAMMACK D. B., HUEHNS E. R., LEHMANN H., SHOOTER E. M. The abnormal polypeptide chains in a number of haemoglobin variants. Acta Genet Stat Med. 1961;11:1–16. doi: 10.1159/000151139. [DOI] [PubMed] [Google Scholar]
- GERALD P. S., DIAMOND L. K. The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin. Blood. 1958 Jan;13(1):61–69. [PubMed] [Google Scholar]
- GOUTTAS A., FESSAS P., TSEVRENIS H., XEFTERI E. Description d'une nouvelle variété d'anémie hémolytique congénitale; etude hématologique, électrophorétique et génétique. Sang. 1955;26(9):911–919. [PubMed] [Google Scholar]
- HEDENBERG F., MULLER-EBERHARD U., SJOLIN S., WRANNE L. Haemoglobin H and inclusion-body anaemia in a Swedish family. Acta Paediatr. 1958 Nov;47(6):652–665. doi: 10.1111/j.1651-2227.1958.tb07681.x. [DOI] [PubMed] [Google Scholar]
- HUISMAN T. H., MARTIS E. A., DOZY A. Chromatography of hemoglobin types on carboxymethylcellulose. J Lab Clin Med. 1958 Aug;52(2):312–327. [PubMed] [Google Scholar]
- HUNT J. A., INGRAM V. M. Abnormal human haemoglobins. IV. The chemical difference between normal human haemoglobin and haemoglobin C. Biochim Biophys Acta. 1960 Aug 26;42:409–421. doi: 10.1016/0006-3002(60)90818-0. [DOI] [PubMed] [Google Scholar]
- HUNT J. A., LEHMANN H. Haemoglobin "Bart's': a foetal haemoglobin without alpha-chains. Nature. 1959 Sep 19;184:872–873. doi: 10.1038/184872a0. [DOI] [PubMed] [Google Scholar]
- INGRAM V. M. Abnormal human haemoglobins. I. The comparison of normal human and sickle-cell haemoglobins by fingerprinting. Biochim Biophys Acta. 1958 Jun;28(3):539–545. doi: 10.1016/0006-3002(58)90516-x. [DOI] [PubMed] [Google Scholar]
- INGRAM V. M. Biochemical genetics at the molecular level. Am J Med. 1963 May;34:674–679. doi: 10.1016/0002-9343(63)90106-2. [DOI] [PubMed] [Google Scholar]
- INGRAM V. M., STRETTON A. O. Genetic basis of the thalassaemia diseases. Nature. 1959 Dec 19;184:1903–1909. doi: 10.1038/1841903a0. [DOI] [PubMed] [Google Scholar]
- ITANO H. A., BERGREN W. R., STURGEON P. The abnormal human hemoglobins. Medicine (Baltimore) 1956 May;35(2):121–159. doi: 10.1097/00005792-195605000-00002. [DOI] [PubMed] [Google Scholar]
- KATZ A. M., DREYER W. J., ANFINSEN C. B. Peptide separation by two-dimensional chromatography and electrophoresis. J Biol Chem. 1959 Nov;234:2897–2900. [PubMed] [Google Scholar]
- KOLER R. D., RIGAS D. A. Genetics of haemoglobin H. Ann Hum Genet. 1961 May;25:95–100. doi: 10.1111/j.1469-1809.1961.tb01503.x. [DOI] [PubMed] [Google Scholar]
- KUNKEL H. G., CEPPELLINI R., MULLER-EBERHARD U., WOLF J. Observations on the minor basic hemoglobin component in the blood of normal individuals and patients with thalassemia. J Clin Invest. 1957 Nov;36(11):1615–1625. doi: 10.1172/JCI103561. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KUNKEL H. G., WALLENIUS G. New hemoglobin in normal adult blood. Science. 1955 Aug 12;122(3163):288–288. doi: 10.1126/science.122.3163.288. [DOI] [PubMed] [Google Scholar]
- LIE-INJO L. E. Alpha-chain thalassemia and hydrops fetalis in Malaya: report of five cases. Blood. 1962 Nov;20:581–590. [PubMed] [Google Scholar]
- MINNICH V., CORDONNIER J. K., WILLIAMS W. J., MOORE C. V. Alpha, beta and gamma hemoglobin polypeptide chains during the neonatal period with description of a fetal form of hemoglobin Da-St. Louis. Blood. 1962 Feb;19:137–167. [PubMed] [Google Scholar]
- MINNICH V., NA-NAKORN S., CHONG-CHAREONSUK S., KOCHASENI S. Mediterranean anemia; a study of thirty-two cases in Thailand. Blood. 1954 Jan;9(1):1–23. [PubMed] [Google Scholar]
- MOTULSKY A. G. Controller genes in synthesis of human haemoglobin. Nature. 1962 May 12;194:607–609. doi: 10.1038/194607b0. [DOI] [PubMed] [Google Scholar]
- MOTULSKY A. G. Genetic and haematological significance of haemoglobin H. Nature. 1956 Nov 10;178(4541):1055–1056. doi: 10.1038/1781055b0. [DOI] [PubMed] [Google Scholar]
- NA-NAKORN S., BANGKOK, THAILAND, MINNICH V., CHERNOFF A. I. Studies on hemoglobin E. II. The incidence of hemoglobin E in Thailand. J Lab Clin Med. 1956 Mar;47(3):490–498. [PubMed] [Google Scholar]
- NEEL J. V., ROBINSON A. R., ZUELZER W. W. Abnormal hemoglobins. Prog Hematol. 1956;1:91–137. [PubMed] [Google Scholar]
- NEEL J. V. The hemoglobin genes: a remarkable example of the clustering of related genetic functions on a single mammalian chromosome. Blood. 1961 Dec;18:769–777. [PubMed] [Google Scholar]
- Nance W. E. Genetic Control of Hemoglobin Synthesis. Science. 1963 Jul 12;141(3576):123–130. doi: 10.1126/science.141.3576.123. [DOI] [PubMed] [Google Scholar]
- PEARSON H. A., McFARLAND W. Erythrokinetics in thalassemia. II. Studies in Lepore trait and hemoglobin H disease. J Lab Clin Med. 1962 Jan;59:147–157. [PubMed] [Google Scholar]
- QUATTRIN N., VENTRUTO V., DINI E., ALOIA L. [On the association of Bart's hemoglobin and microcythemia. First Italian case]. Minerva Med. 1961 Sep 19;52:3189–3197. [PubMed] [Google Scholar]
- RAMOT B., SHEBA C., FISHER S., AGER J. A., LEHMANN H. Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin. Br Med J. 1959 Dec 5;2(5161):1228–1230. doi: 10.1136/bmj.2.5161.1228. [DOI] [PMC free article] [PubMed] [Google Scholar]
- RIGAS D. A., KOLER R. D., OSGOOD E. E. Hemoglobin H; clinical, laboratory, and genetic studies of a family with a previously undescribed hemoglobin. J Lab Clin Med. 1956 Jan;47(1):51–64. [PubMed] [Google Scholar]
- SINGER K., CHERNOFF A. I., SINGER L. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation. Blood. 1951 May;6(5):413–428. [PubMed] [Google Scholar]
- SMITH E. W., CONLEY C. L. Filter paper electrophoresis of human hemoglobins with special reference to the incidence and clinical significance of hemoglobin C. Bull Johns Hopkins Hosp. 1953 Aug;93(2):94–106. [PubMed] [Google Scholar]
- Singer S. J., Itano H. A. ON THE ASYMMETRICAL DISSOCIATION OF HUMAN HEMOGLOBIN. Proc Natl Acad Sci U S A. 1959 Feb;45(2):174–184. doi: 10.1073/pnas.45.2.174. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TUCHINDA S., VAREENIL C., BHANCHIT P., MINNICH V. Fast hemoglobin component found in umbilical-cord blood of Thai babies. Pediatrics. 1959 Jul;24(1):43–49. [PubMed] [Google Scholar]
- VELLA F., WELLS R. H., AGER J. A., LEHMANN H. A haemoglobinopathy involving haemoglobin H and a new (Q) haemoglobin. Br Med J. 1958 Mar 29;1(5073):752–755. doi: 10.1136/bmj.1.5073.752. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WOLFF J. A., MICHAELS R. H., VON HOFF F. H. Hemoglobin H-thalassemia disease. Blood. 1958 May;13(5):492–501. [PubMed] [Google Scholar]
- ZUELZER W. W., KAPLAN E. Thalassemia-hemoglobin C disease; a new syndrome presumably due to the combination of the genes for thalassemia and hemoglobin C. Blood. 1954 Nov;9(11):1047–1054. [PubMed] [Google Scholar]